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NCT05488847 · ClinicalTrials.gov registry record · Phase 4

Opioid-Free Pain Protocol After Shoulder Arthroplasty

A Phase 4 study of Shoulder Pain and Shoulder Arthropathy, sponsored by Henry Ford Health System.

Active
Registry status
Phase 4
Development phase
83
Enrollment target
1
Study location

NCT05488847: Active Phase 4 study of Shoulder Pain and Shoulder Arthropathy, sponsored by Henry Ford Health System.

NCT05488847 is a Phase 4 study of Shoulder Pain and Shoulder Arthropathy that is active but no longer recruiting, run by Henry Ford Health System. The registered enrollment target is 83 participants, below the 98-participant average among 27 other Shoulder Pain trials with a reported enrollment target (15% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05488847, a Phase 4 study of Shoulder Pain and Shoulder Arthropathy, is active but no longer recruiting, sponsored by Henry Ford Health System.

ACTIVE NOT RECRUITING
Registry status
Phase 4
Development phase
83 participants
Enrollment target
1
Study location

Study Summary

This randomized, single blinded, clinical trial aims to investigate the efficacy of a multimodal pain control regimen for shoulder arthroplasty. Patients who receive a multimodal pain control regimen alone (study group) will be compared to patients who receive a multimodal pain control regimen plus a standard prescription of an opioid containing medication (comparison group). The primary outcome is average daily Numerical Rating Scale (NRS) pain score in the first 10 days after surgery. We hypothesize that there will be no significant difference in the primary outcome between the two groups.

Primary Outcome

Patients record pain levels using a Visual analog scale for 10 days post-operatively. On each day, patients report their pain level via an automated text messaging service in the morning, afternoon, and the evening. A mean pain level is calculated from all scores reported by a patient in the first 10 days postoperatively. Patients will use a 0-10 scale along with visuals to indicate their level of pain with 0 being no pain at all and 10 being the worst pain possible. Lower scores indicate better

Interventions

  • DRUG Acetaminophen
  • DRUG Dexamethasone
  • DRUG Celecoxib
  • DRUG Tramadol
  • DRUG Pregabalin

Study Locations (1)

Michigan

  • Henry Ford Health - Detroit

Trial Details

FieldValue
Enrollment Target 83 participants
Start Date 2022-06-25
Est. Completion 2026-09-01
Phase Phase 4
Henry Ford Health System

234 total trials

What the registry record for NCT05488847 still lists

NCT05488847 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 83 participants, a relatively small participant target, below the 98-participant average among 27 other Shoulder Pain trials with a reported enrollment target (15% lower).

The record links to 2 conditions, with Shoulder Pain appearing as the primary indexed condition, and to 5 interventions - of which Acetaminophen is the first listed.

NCT05488847 reports a single indexed study location in Michigan.

Frequently Asked Questions

What is clinical trial NCT05488847 about?

NCT05488847 is a clinical study titled "Opioid-Free Pain Protocol After Shoulder Arthroplasty". This randomized, single blinded, clinical trial aims to investigate the efficacy of a multimodal pain control regimen for shoulder arthroplasty. Patients who receive a multimodal pain control regimen alone (study group) will be compared to patients who receive a multimodal pain control regimen plus ...

What is the current status of trial NCT05488847?

This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 83 participants. The study started on 2022-06-25. Estimated completion is 2026-09-01.

What conditions does trial NCT05488847 study?

This clinical trial studies the following conditions: Shoulder Pain, Shoulder Arthropathy.

What interventions are being tested in trial NCT05488847?

The interventions under investigation include: Acetaminophen (DRUG), Dexamethasone (DRUG), Celecoxib (DRUG), Tramadol (DRUG), Pregabalin (DRUG).

Who is sponsoring clinical trial NCT05488847?

This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05488847 being conducted?

This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Shoulder Pain

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05488847's enrollment target sits among peer trials

83 11th of 27 higher than 17 of 27 other Shoulder Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Shoulder Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05488847, the US trial registry maintained by the National Library of Medicine. NCT05488847 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.